Antibodies to the pcrv antigen of pseudomonas aeruginosa

ABSTRACT

The current invention provides high-affinity antibodies to the  Pseudomonas aeruginosa  PcrV protein that have reduced immunogenicity when administered to treat  Pseudomonas aeruginosa  infections.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 13/271,146, filed Oct. 11, 2011, which is a continuation of U.S. application Ser. No. 12/325,806, filed Dec. 1, 2008, which claims benefit of U.S. provisional application No. 60/991,679, filed Nov. 30, 2007, each of which applications is herein incorporated by reference.

REFERENCE TO A SEQUENCE LISTING SUBMITTED AS AN ASCII TEXT FILE

The sequence listing written in file 87142_(—)920734_seq_(—)1st.txt, created on Oct. 1, 2014, 68,597 bytes, machine format IBM-PC, MS-Windows operating system, is herein incorporated by reference.

BACKGROUND OF THE INVENTION

Pseudomonas aeruginosa (P. aeruginosa) is an opportunistic pathogen that rarely causes disease in healthy people, but is a significant problem for critically ill or immunocompromised individuals. Infection is a major problem in individuals who have cystic fibrosis (CF), where P. aeorginosa is a causative agent in the progressive loss of lung function resulting from recurrent and chronic respiratory tract infections with the bacterium. Others at risk from Pseudomonas aeruginosa infection include patients on mechanical ventilators, neutropenic cancer patients, and burn patients. P. aeruginosa is often resistant to most antibiotics and new treatment approaches are greatly needed.

The type III secretion system is an important virulence factor determinant in that it inhibits host defense system. Upon activation, the type III secretion apparatus translocates toxins into the cytoplasm of the host cell, resulting in cell rounding, lifting, and cell death by necrosis or apoptosis. PcrV is an essential component of the type III secretion apparatus. Blocking of PcrV can inhibit toxin secretion through the Type III secretion system, thereby allowing natural clearance mechanisms to eliminate the bacteria. PcrV is conserved in all P. aeruginosa strains tested thus far.

Antibodies to the PcrV antigen of Pseudomonas are known in the art. The current invention provides improved PcrV antibodies, e.g., for the treatment of Pseudomonas aeruginosa infections.

BRIEF SUMMARY OF THE INVENTION

The current invention relates to engineered antibodies that bind with high affinity, e.g., at about 50 nM, or about 10 nM or less, to the PcrV antigen from Pseudomonas aeruginosa. Such antibodies are often functional antagonists of the Type III secretion, i.e., the antibody binds to PcrV and inhibits the Type III secretion system. In some embodiments, an antibody of the invention may bind to PcrV and recruit multiple cell types of the immune system to stimulate phagocytosis by macrophages, antibody directed cellular cytotoxicity (ADCC) by macrophages or NK cells, activation of the complement cascade, and/or generation of the oxidative burst by neutrophils.

The antibodies of the invention have variable regions with a high degree of identity to human germ-line V_(H) and V_(L) sequences and are less immunogenic in humans. The CDR3 sequences of the heavy and light chains of the present invention comprise a pair of binding specificity determinants (BSD) from the monoclonal anti-PcrV antibody Mab166 (Frank et al., J. Infectious Dis. 186: 64-73, 2002). The antibodies of the invention typically are capable of competing with Mab166 for binding to a neutralizing epitope on the PcrV protein.

The BSD sequence in CDRH3 has the amino acid sequence NRGDIYYDFTY (SEQ ID NO:38). The BSD in CDRL3 is FWXTP (where X may be either S or G; SEQ ID NO:39). Complete V-regions are generated in which the BSD forms part of the CDR3 and additional sequences are used to complete the CDR3 and add a FR4 sequence. Typically, the portion of the CDR3 excluding the BSD and the complete FR4 are comprised of human germ-line sequences. Preferably, the CDR3-FR4 sequence excluding the BSD differs from human germ-line sequences by not more than two amino acids on each chain. The CDR3-FR4 is joined to a V-segment that has a high degree identity, e.g., at least 80%, or at least 90%, or more to a human germline V segment.

In some aspects, the invention provides an anti-PcrV antibody that exhibits high affinity binding, e.g., 10 nM or better, to PcrV and is an antagonist of the Type III secretion system.

In many embodiments, an anti-PcrV antibody of the invention that selectively binds to PcrV comprises: a V_(L) region that comprises a CDR3 comprising FWGTP. In typical embodiments, such an antibody has a V_(L) region V-segment has at least 80% identity to a human germline V-segment. The FR4 region typically has at least 90% identity to the FR4 region of a human germline J segment.

In some embodiments, an anti-PcrV antibody of the invention comprises a CDR3 comprising FWGTP (SEQ ID NO:40), a FR4 and a V-segment, wherein the FR4 comprises at least 90% identity to the FR4 region of the human JK2 germline gene segment or at least 90% identity to the JL2 germline sequence; and the V-segment comprises at least 80% identity to a human germline Vkappa I or Vkappa III sequence, or at least 80% identity to a human germline Vlambda sequence. In some embodiments the V_(L) region CDR3 has the sequence Q(Q/H)FWGTPYT (SEQ ID NO:41). In some embodiments, the antibody further comprises a V_(H) region that comprises a CDR3 having a sequence NRGDIYYDFTY (SEQ ID NO:38), a FR4 and a V-segment, wherein the FR4 comprises at least 90% identity to the FR4 region of the human JH3 or human JH6 segment and the V-segment comprises at least 80% identity to the human VH1-18 subclass V-segment or to the human VH3-30.3 V segment. In some embodiments, the V_(H) region comprises a CDR3 having a sequence NRGDIYYDFTYA(M/F)DX₁ (SEQ ID NO:42), wherein X₁ is I, Q, Y, or S.

In further embodiments, the invention provides an anti-PcrV antibody that binds to PcrV, comprising: a V_(H) region that comprises a CDR3 having a sequence NRGDIYYDFTYAMDX₁ (SEQ ID NO:43), wherein X₁ is I, Q, Y, or S; a FR4 and a V-segment, wherein the FR4 comprises at least 90% identity to the FR4 region of the human germline JH3 segment or the FR4 region of the human germine JH6 segment, and the V-segment comprises at least 80% identity to the human germline VH1-18 subclass V-segment or to the human germline VH3-30.3 subclass V segment, with the proviso that when X₁ is Y, the FR4 region is not WGQGTSVTVSS (SEQ ID NO:44).

In some embodiments, the invention provides an anti-PcrV antibody that binds to PcrV, comprising: a V_(H) region that comprises a CDR3 having a sequence NRGDIYYDFTYAMDX₁ (SEQ ID NO:43), wherein X₁ is I, Q, Y, or S; a FR4 and a V-segment, wherein the FR4 comprises at least 90% identity to the FR4 region of the human germline JH3 segment or the FR4 region of the human germline JH6 segment, and the V-segment comprises at least 80% identity to the human germline VH1-18 subclass V-segment or to the human germline VH3-30.3 subclass V segment, with the proviso that when X₁ is Y, the FR4 region is not WGQGTSVTVSS (SEQ ID NO:44); and a V_(L) region that comprises a CDR3 comprising FW(S/G)TP (SEQ ID NO:39), a FR4 and a V-segment, wherein the FR4 comprises at least 90% identity to the FR4 region of the human germline JK2 gene segment or to the FR4 region of the human germline JL2 segment; and the V-segment comprises at least 80% identity to the human germline VKI L12 sequence, or at least 80% identity to a Vkappa III sequence, or at least 80% identity to a human germline Vlambda2 2c or Vlambda3 31 segment.

In some embodiment, the FR4 of the V_(H) region of an antibody of the invention has the sequence WGQGTX₂VTVSS (SEQ ID NO:45), wherein X₂ is T or M.

In some embodiments, an antibody of the invention has a light chain CDR3 that has the sequence Q(H/Q)FW(G/S)TPYT (SEQ ID NO:46).

In some embodiments, the FR4 of the V_(L) region has the sequence FGQGTKLEIK (SEQ ID NO:47) or FGGGTKLTVL (SEQ ID NO:48).

The invention also provides an anti-PcrV antibody where the V_(H) region V-segment has at least 80% identity to the human germline VH3-30.3 segment and the heavy chain region CDR1 comprises the sequence X₃X₄X₅X₆H, wherein X₃ is S, T, or N; X₄ is Y or A; X₅ is A, G, or P; and X₆ is M, I, or L; and the heavy chain region CDR2 comprises the sequence X₇IX₈YX₉GX₁₀X₁₁X₁₂X₁₃Y(A/I)X₁₄SVKG (SEQ ID NO:49), wherein X₇ is V, F, or N; X₈ is S or W; X₉ is D or N; X₁₀ is S, K, R or Y; X₁₁ is N, S, D or E; X₁₂ is K, I, or E; X₁₃ is Y, S, D or W; and X₁₄ is D or S. In some embodiments, the antibody has at least 90% identity to a VH3-30.3 V segment. In some embodiments, the CDR1 is TAGMH (SEQ ID NO:50), SYGIH (SEQ ID NO:51), SYGMH (SEQ ID NO:52), SYPLH (SEQ ID NO:53), or NYPMH (SEQ ID NO:54). In some embodiments, the CDR2 is VIWYNGKEISYADSVKG (SEQ ID NO:55), FISYDGSEKYYASSVKG (SEQ ID NO:56), VISYDGSEKWYADSVKG (SEQ ID NO:57), VIWYDGRNKYYADSVKG (SEQ ID NO:58), VIWYDGYNKDYADSVKG (SEQ ID NO:59), or NIWYDGSSESYIDSVKG (SEQ ID NO:60). In some embodiments, the CDR1 is TAGMH (SEQ ID NO:50), SYGIH (SEQ ID NO:51), SYGMH (SEQ ID NO:52), SYPLH (SEQ ID NO:53), or NYPMH (SEQ ID NO:54); and the CDR2 is VIWYNGKEISYADSVKG (SEQ ID NO:55), FISYDGSEKYYASSVKG (SEQ ID NO:56), VISYDGSEKWYADSVKG (SEQ ID NO:57), VIWYDGRNKYYADSVKG (SEQ ID NO:58), VIWYDGYNKDYADSVKG (SEQ ID NO:59), or NIWYDGSSESYIDSVKG (SEQ ID NO:60).

The invention also provides an anti-PcrV antibody where the V_(H) region V-segment has at least 80% identity, or at least 90% identity, to the human germline VH1-18 sub-class V-segment and the CDR1 has the sequence DHAIS (SEQ ID NO:61) and the CDR2 has the sequence WISPYSGNPNYAQSLQG (SEQ ID NO:62).

The invention also provides an anti-PcrV antibody that binds to PcrV, comprising: a VH region that has a CDR3 sequence NRGDIYYDFTYAFDI (SEQ ID NO:63), a CDR1 sequence DHAIS (SEQ ID NO:61) and a CDR2 sequence WISPYSGNPNYAQSLQG (SEQ ID NO:62).

In some embodiments the V_(H) region comprises the V-segment region of an amino acid sequence selected from the group consisting of SEQ ID NOS:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 26, 27, 29, and 35. For example, the V_(H) regions can comprise an amino acid sequence selected from the group consisting of SEQ ID NOS:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 26, 27, 29, and 35.

The invention also provides an anti-PcrV where the V_(L) region V-segment comprises at least 80% or 90% identity, to a human germline Vkappa I L12 or Vkappa III sequence; or at least 80% or 90% identity to a human germline Vlambda3 31 or to a Vlambda2 2c sequence. In some embodiments, V_(L) region V-segment has at least 80% or 90% identity to the human germline VKI L12 segment and the CDR1 has the sequence RASX₁₅X₁₆X₁₇X₁₈X₁₉X₂₀X₂₁A (SEQ ID NO:64), where X₁₅ is Q or E; X₁₆ is S or G; X₁₇ is I or V; X₁₈ is S or D; X₁₉ is S, R, or T; X₂₀ is W or Y; and X₂₁ is L or V; and the CDR2 has the sequence X₂₁ASX₂₂LX₂₃S (SEQ ID NO:65), wherein X₂₁ is D or A; X₂₂ is S, A, or T; and X₂₃ is E, Q, or K. In some embodiments, the CDR1 has the sequence RASQGISTYLA (SEQ ID NO:66), RASQGISSWLA (SEQ ID NO:67), RASQSISRWVA (SEQ ID NO:68), or RASEGVDRWLA (SEQ ID NO:69); or the CDR2 has the sequence AASSLQS (SEQ ID NO:70), DASSLKS (SEQ ID NO:71), DASALQS (SEQ ID NO:72), or DASTLQS (SEQ ID NO:73). In some embodiments, the CDR1 has the sequence RASQGISTYLA (SEQ ID NO:66), RASQGISSWLA (SEQ ID NO:67), RASQSISRWVA (SEQ ID NO:68), or RASEGVDRWLA (SEQ ID NO:69); and the CDR2 has the sequence AASSLQS (SEQ ID NO:70), DASSLKS (SEQ ID NO:71), DASALQS (SEQ ID NO:72), or DASTLQS (SEQ ID NO:73).

The invention also provides an anti-PcrV antibody where the V_(L) region V segment has at least 80%, or at least 90%, amino acid sequence identity to the human germline VKIII L2 sequence and the CDR1 has the sequence RASNSVGAYNLA (SEQ ID NO:74) or RASQSVSSNLA (SEQ ID NO:75); or the CDR2 has the sequence (A/G)AS(T/R)RA(T/P) (SEQ ID NO:76). In some embodiments, CDR1 has the sequence RASNSVGAYNLA (SEQ ID NO:74) or RASQSVSSNLA (SEQ ID NO:75); and the CDR2 has the sequence (A/G)AS(T/R)RA(T/P) (SEQ ID NO:76).

Further, the invention provides an anti-PcrV antibody where the V_(L) region V-segment has at least 80%, or at least 90%, amino acid sequence identity to a human germline Vlambda L3 31 segment and the CDR1 has the sequence QGDSLRS(Y/L)YAS (SEQ ID NO:77); or the CDR2 has the sequence (G/S)KN(N/S)RPS (SEQ ID NO:78). In some embodiments, the CDR1 has the sequence QGDSLRS(Y/L)YAS (SEQ ID NO:77); and the CDR2 has the sequence (G/S)KN(N/S)RPS (SEQ ID NO:78).

In some embodiments, the invention provide an anti-PcrV antibody where the V_(L) region V-segment has at least 80%, or at least 90%, amino acid sequence identity to a human germline Vlambda L2 2c segment and the CDR1 has the sequence TGTSSDVGAYNYVS (SEQ ID NO:79) or TGTSSDYVS (SEQ ID NO:80); or the CDR2 has the sequence (E/D)VT(K/N)RPS (SEQ ID NO:81). In some embodiments, the CDR1 has the sequence TGTSSDVGAYNYVS (SEQ ID NO:79) or TGTSSDYVS (SEQ ID NO:80); and the CDR2 has the sequence (E/D)VT(K/N)RPS (SEQ ID NO:81).

An anti-PcrV antibody of the invention can have a region that comprises the V-segment of an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 28, 30, 32, 34, 36, and 37. For example the V_(L) region can comprise an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 28, 30, 32, 34, 36, and 37.

The invention thus provides an anti-PcrV antibody that comprises: a V_(H) region having an amino acid sequence selected from the group consisting of SEQ ID NOS:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 26, 27, 29, and 35; and a V_(L) region having an amino acid sequence selected from the group consisting of SEQ ID NO:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 28, 30, 32, 34, 36, and 37. Thus, in some embodiments, an antibody of the invention comprises a V_(H) region of SEQ ID NO:1 and a V_(L) region of SEQ ID NO:2; or a V_(H) region of SEQ ID NO:3 and a V_(L) region of SEQ ID NO:4; or a V_(H) region of SEQ ID NO:5 and a V_(L) region of SEQ ID NO:6; or a V_(H) region of SEQ ID NO:7 and a V_(L) region of SEQ ID NO:8; or a V_(H) region of SEQ ID NO:11 and a V_(L) region of SEQ ID NO:12; or a V_(H) region of SEQ ID NO:9 and a V_(L) region of SEQ ID NO:10; or a V_(H) region of SEQ ID NO:13 and a V_(L) region of SEQ ID NO:10; or a V_(H) region of SEQ ID NO:13 and a V_(L) region of SEQ ID NO:4; or a V_(H) region of SEQ ID NO:13 and a V_(L) region of SEQ ID NO:37; or a V_(H) region of SEQ ID NO:21 and a V_(L) region of SEQ ID NO:18; or a V_(H) region of SEQ ID NO:17 and a V_(L) region of SEQ ID NO:18; or a V_(H) region of SEQ ID NO:26 and a V_(L) region of SEQ ID NO:24; or a V_(H) region of SEQ ID NO:25 and a V_(L) region of SEQ ID NO:24; or a V_(H) region of SEQ ID NO:23 and a V_(L) region of SEQ ID NO:24; or a V_(H) region of SEQ ID NO:35 and a V_(L) region of SEQ ID NO:36; or V_(H) region of SEQ ID NO:29 and a V_(L) region of SEQ ID NO:20; or V_(H) region of SEQ ID NO:29 and a V_(L) region of SEQ ID NO:28; or a V_(H) region of SEQ ID NO:29 and a V_(L) region of SEQ ID NO:30; or a V_(H) region of SEQ ID NO:29 and a V_(L) region of SEQ ID NO:34; or a V_(H) region of SEQ ID NO:3 and a V_(L) region of SEQ ID NO:32.

In some embodiments, an anti-PcrV antibody of the invention comprises a heavy chain as set forth in FIG. 1 and/or a light chain as set forth in FIG. 2; or has at least one, often at least two, and in some embodiments, at least three CDRs from one of the heavy or light chains set forth in FIG. 1 or FIG. 2, respectively. In many embodiments, the CDR1 and/or CDR2 sequence is not a germline sequence.

In some embodiments, the antibody is a Fab′ fragment.

In some embodiments, an antibody of the invention is a Fab, or Fab′, that has an affinity of about 10 nM or less. In some embodiments, the antibody has an affinity that is equal or better than, the affinity of a Mab166 Fab or Fab′.

The potency of an antibody of the invention, e.g., a Fab, in inhibiting the activity of the P. aeruginosa Type III Secretion System is typically equivalent to Mab 166 Fab (within two-fold of the activity in cell-based assays). In some embodiments, an antibody of the invention is more potent than Mab 166 in preventing cytotoxicity by P. aeruginosa.

In some embodiments, the antibody comprises a hinge region.

In other embodiments, the antibody is an IgG or an IgA.

In some embodiments, the antibody is PEGylated. For example, the antibody can be di-PEGylated.

In some embodiments, the V_(H) region or the V_(L) region, or both the V_(H) and V_(L) region amino acid sequences comprise a methionine at the N-terminus.

In a further aspect, the invention provides a method of treating a patient infected with P. aeruginosa, the method comprising administering a therapeutically effective amount of an antibody as described herein. In some embodiments, the antibody is administered intravenously, subcutaneously, or by insufflation.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows sequences of V_(H) regions of anti-PcrV antibodies (SEQ ID NOS:1, 7, 9, 5, 11, 3, 19, 19, 19, 13, 15, 17, 21, 23, 25, 26 and 35, respectively). CDR sequences are underlined. The VH1 sequence is aligned to human germ-line sequence VH1-18 (SEQ ID NO:82). VH3-subclass antibodies are shown aligned to human germ-line sequence VH3-30.3 (SEQ ID NO:83). J-segments are aligned to either human germ-line JH3 or JH6 (SEQ ID NO:84). The V_(H)-segments depicted in FIG. 1 correspond to the sequence up to the CDR3 sequence.

FIG. 2 shows sequences of V_(L) regions of anti-PcrV antibodies (SEQ ID NOS:24, 2, 8, 10, 10, 6, 12, 4, 37, 36, 87, 18, 20, 18, 30, 32, 90 and 28, respectively). CDR sequences are underlined. Vkappa-subclass antibodies are shown aligned to human germline sequence VkI L12 (SEQ ID NO:85) or VkIII L2 (SEQ ID NO:86). J-segments are aligned to human germ-line Jk2. Vlambda-subclass antibodies are shown aligned to human germline sequence VL3 31 (SEQ ID NO:88) or VL2 2c (SEQ ID NO:89). J-segments are aligned to human germ-line J12.

FIG. 3 shows an exemplary constant region sequence that can be linked to Fab′ Heavy (SEQ ID NO:91) and Light (SEQ ID NO:92) Chains. The two cysteine residues in the hinge region available for conjugation of thiol-reactive maleimide derivatives are underlined. The cysteine residues involved in formation of an interchain disulfide bond are boxed.

FIG. 4 shows a schematic representation of the structure of a di-PEGylated Fab′ in which two molecules of mPEG-maleimide are conjugated via thioether linkages to cysteine residues in the hinge region of the Fab′ protein. The exemplary antibody is comprised of a human Fd′ heavy chain and human kappa light chain linked by a disulphide bond represented by the cross-bar between the two chains. (Fab and PEG components are not to scale.)

FIG. 5A-5H provides data showing a time course of survival of mice treated with various doses of antibodies to PcrV at the time of challenge with a lethal dose of PA103. Mab166 and Fab fragments were co-instilled via the intratracheal route with 1.5×106 bacteria (5 mice per group, 4 mice for Mab166 Fab groups). Control is a nonspecific Fab with no binding to PcrV or any P. aeruginosa protein. Mice were treated with antibody doses of: 5A) 10 μg, 5B) 5 μg, 5C) 2.5 μg, 5D) 1.25 μg, *P=0.01 for Fab 1A8 vs. Mab166 Fab, 5E) 0.625 μg *P=0.002 for 1A8 vs. Mab166 Fab, 5F) 0.3125 μg, 5G) 0.16 μg, 5H) 0.08 μg. P values for differences between treatment groups determined by Mantel-Cox log-rank test.

FIG. 6A-6F provides data showing a body temperature analysis of mice treated with anti-PcrV antibodies. Rectal temperatures are shown for 48 hours or until mortality. Antibody doses: 6A) 10 μg, 6B) 5 μg, 6C) 2.5 μg, 6D) 1.25 μg, 6E) 0.625 μg, 6F) 0.3125 μg.

FIG. 7 provides data showing clearance of P. aeruginosa from the lungs of infected mice by anti-PcrV antibodies. Mice were infected with 1.5×10⁶ cfu PA103 co-instilled with Mab 166 IgG, Mab 166 Fab or human Fab 1A8 at the doses shown (in μg). The graph shows cfu/lung isolated from individual mice surviving at 48 h. The number of dead mice at this time point is shown above the figure. Median cfu/lung for surviving mice in each group is shown with a bar.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, an “antibody” refers to a protein functionally defined as a binding protein and structurally defined as comprising an amino acid sequence that is recognized by one of skill as being derived from the framework region of an immunoglobulin-encoding gene of an animal that produces antibodies. An antibody can consist of one or more polypeptides substantially encoded by immunoglobulin genes or fragments of immunoglobulin genes. The recognized immunoglobulin genes include the kappa, lambda, alpha, gamma, delta, epsilon and mu constant region genes, as well as myriad immunoglobulin variable region genes. Light chains are classified as either kappa or lambda. Heavy chains are classified as gamma, mu, alpha, delta, or epsilon, which in turn define the immunoglobulin classes, IgG, IgM, IgA, IgD and IgE, respectively.

A typical immunoglobulin (antibody) structural unit is known to comprise a tetramer. Each tetramer is composed of two identical pairs of polypeptide chains, each pair having one “light” (about 25 kD) and one “heavy” chain (about 50-70 kD). The N-terminus of each chain defines a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition. The terms variable light chain (V_(L)) and variable heavy chain (V_(H)) refer to these light and heavy chains, respectively.

The term “antibody” as used herein includes antibody fragments that retain binding specificity. For example, there are a number of well characterized antibody fragments. Thus, for example, pepsin digests an antibody below the disulfide linkages in the hinge region to produce F(ab)′₂, a dimer of Fab which itself is a light chain joined to VH-CH1 (Fd) by a disulfide bond. The F(ab)′₂ may be reduced under mild conditions to break the disulfide linkage in the hinge region thereby converting the (Fab′)₂ dimer into an Fab′ monomer. The Fab′ monomer is essentially a Fab with all or part of the hinge region (see, Fundamental Immunology, W. E. Paul, ed., Raven Press, N.Y. (1993), for a more detailed description of other antibody fragments). While various antibody fragments are defined in terms of the digestion of an intact antibody, one of skill will appreciate that fragments can be synthesized de novo either chemically or by utilizing recombinant DNA methodology. Thus, the term antibody, as used herein also includes antibody fragments either produced by the modification of whole antibodies or synthesized using recombinant DNA methodologies.

Antibodies of the invention include dimers such as V_(H)-V_(L) dimers, V_(H) dimers, or V_(L) dimers, including single chain antibodies (antibodies that exist as a single polypeptide chain), such as single chain Fv antibodies (sFv or scFv) in which a variable heavy and a variable light region are joined together (directly or through a peptide linker) to form a continuous polypeptide. The single chain Fv antibody is a covalently linked V_(H)-V_(L) heterodimer which may be expressed from a nucleic acid including V_(H)- and V_(L)-encoding sequences either joined directly or joined by a peptide-encoding linker (e.g., Huston, et al. Proc. Nat. Acad. Sci. USA, 85:5879-5883, 1988). While the V_(H) and V_(L) are connected to each as a single polypeptide chain, the V_(H) and V_(L) domains associate non-covalently. Alternatively, the antibody can be another fragment, such as a disulfide-stabilized Fv (dsFv). Other fragments can also be generated, including using recombinant techniques. The scFv antibodies and a number of other structures converting the naturally aggregated, but chemically separated light and heavy polypeptide chains from an antibody V region into a molecule that folds into a three dimensional structure substantially similar to the structure of an antigen-binding site are known to those of skill in the art (see e.g., U.S. Pat. Nos. 5,091,513, 5,132,405, and 4,956,778). In some embodiments, antibodies include those that have been displayed on phage or generated by recombinant technology using vectors where the chains are secreted as soluble proteins, e.g., scFv, Fv, Fab, (Fab′)₂ or generated by recombinant technology using vectors where the chains are secreted as soluble proteins. Antibodies for use in the invention can also include diantibodies and miniantibodies.

Antibodies of the invention also include heavy chain dimers, such as antibodies from camelids. Since the V_(H) region of a heavy chain dimer IgG in a camelid does not have to make hydrophobic interactions with a light chain, the region in the heavy chain that normally contacts a light chain is changed to hydrophilic amino acid residues in a camelid. V_(H) domains of heavy-chain dimer IgGs are called VHH domains. Antibodies of the invention include single domain antibodies (dAbs) and nanobodies (see, e.g., Cortez-Retamozo, et al., Cancer Res. 64:2853-2857, 2004).

As used herein, “V-region” refers to an antibody variable region domain comprising the segments of Framework 1, CDR1, Framework 2, CDR2, and Framework 3, including CDR3 and Framework 4, which segments are added to the V-segment as a consequence of rearrangement of the heavy chain and light chain V-region genes during B-cell differentiation. A “V-segment” as used herein refers to the region of the V-region (heavy or light chain) that is encoded by a V gene. The V-segment of the heavy chain variable region encodes FR1-CDR1-FR2-CDR2 and FR3. For the purposes of this invention, the V-segment of the light chain variable region is defined as extending though FR3 up to CDR3.

As used herein, the term “J-segment” refers to a subsequence of the variable region encoded comprising a C-terminal portion of a CDR3 and the FR4. An endogenous J-segment is encoded by an immunoglobulin J-gene.

As used herein, “complementarity-determining region (CDR)” refers to the three hypervariable regions in each chain that interrupt the four “framework” regions established by the light and heavy chain variable regions. The CDRs are primarily responsible for binding to an epitope of an antigen. The CDRs of each chain are typically referred to as CDR1, CDR2, and CDR3, numbered sequentially starting from the N-terminus, and are also typically identified by the chain in which the particular CDR is located. Thus, for example, a V_(H) CDR3 is located in the variable domain of the heavy chain of the antibody in which it is found, whereas a V_(L) CDR1 is the CDR1 from the variable domain of the light chain of the antibody in which it is found.

The sequences of the framework regions of different light or heavy chains are relatively conserved within a species. The framework region of an antibody, that is the combined framework regions of the constituent light and heavy chains, serves to position and align the CDRs in three dimensional space.

The amino acid sequences of the CDRs and framework regions can be determined using various well known definitions in the art, e.g., Kabat, Chothia, international ImMunoGeneTics database (IMGT), and AbM (see, e.g., Johnson et al., supra; Chothia & Lesk, 1987, Canonical structures for the hypervariable regions of immunoglobulins. J. Mol. Biol. 196, 901-917; Chothia C. et al., 1989, Conformations of immunoglobulin hypervariable regions. Nature 342, 877-883; Chothia C. et al., 1992, structural repertoire of the human VH segments J. Mol. Biol. 227, 799-817; Al-Lazikani et al., J. Mol. Biol 1997, 273(4)). Definitions of antigen combining sites are also described in the following: Ruiz et al., IMGT, the international ImMunoGeneTics database. Nucleic Acids Res., 28, 219-221 (2000); and Lefranc, M.-P. IMGT, the international ImMunoGeneTics database. Nucleic Acids Res. Jan 1; 29(1):207-9 (2001); MacCallum et al, Antibody-antigen interactions: Contact analysis and binding site topography, J. Mol. Biol., 262 (5), 732-745 (1996); and Martin et al, Proc. Natl Acad. Sci. USA, 86, 9268-9272 (1989); Martin, et al, Methods Enzymol., 203, 121-153, (1991); Pedersen et al, Immunomethods, 1, 126, (1992); and Rees et al, In Sternberg M. J. E. (ed.), Protein Structure Prediction. Oxford University Press, Oxford, 141-172 1996).

“Epitope” or “antigenic determinant” refers to a site on an antigen to which an antibody binds. Epitopes can be formed both from contiguous amino acids or noncontiguous amino acids juxtaposed by tertiary folding of a protein. Epitopes formed from contiguous amino acids are typically retained on exposure to denaturing solvents whereas epitopes formed by tertiary folding are typically lost on treatment with denaturing solvents. An epitope typically includes at least 3, and more usually, at least 5 or 8-10 amino acids in a unique spatial conformation. Methods of determining spatial conformation of epitopes include, for example, x-ray crystallography and 2-dimensional nuclear magnetic resonance. See, e.g., Epitope Mapping Protocols in Methods in Molecular Biology, Vol. 66, Glenn E. Morris, Ed (1996).

The term “binding specificity determinant” or “BSD” as used in the context of the current invention refers to the minimum contiguous or non-contiguous amino acid sequence within a CDR region necessary for determining the binding specificity of an antibody. In the current invention, the minimum binding specificity determinants reside within a portion or the full-length of the CDR3 sequences of the heavy and light chains of the antibody.

As used herein, the terms “PcrV antagonizing antibody” or an “anti-PcrV antibody is an antagonist of the Pseudomonas aeruginosa Type III secretion system” are used interchangeably to refer to an antibody that binds to PcrV and inhibits the Type III secretion system Inhibition occurs when secretion through the Type III secretion system is at least about 10% less, for example, at least about 25%, 50%, 75% less, or totally inhibited, in comparison to secretion when not exposed to the antibody antagonist. The terms “anti-PcrV antibody” and “PcrV antibody” are used synonymously unless otherewise stated.

The term “equilibrium dissociation constant (K_(D)) refers to the dissociation rate constant (k_(d), time⁻¹) divided by the association rate constant (k_(a), time⁻¹, M⁻¹). Equilibrium dissociation constants can be measured using any known method in the art. The antibodies of the present invention are high affinity antibodies. Such antibodies have an affinity better than 500 nM, and often better than 50 nM or 10 nM. Thus, in some embodiments, the antibodies of the invention have an affinity in the range of 500 nM to 100 pM, or in the range of 50 or 25 nM to 100 pM, or in the range of 50 or 25 nM to 50 pM, or in the range of 50 nM or 25 nM to 1 pM.

As used herein, “humanized antibody” refers to an immunoglobulin molecule in CDRs from a donor antibody are grafted onto human framework sequences. Humanized antibodies may also comprise residues of donor origin in the framework sequences. The humanized antibody can also comprise at least a portion of a human immunoglobulin constant region. Humanized antibodies may also comprise residues which are found neither in the recipient antibody nor in the imported CDR or framework sequences. Humanization can be performed using methods known in the art (e.g., Jones et al., Nature 321:522-525; 1986; Riechmann et al., Nature 332:323-327, 1988; Verhoeyen et al., Science 239:1534-1536, 1988); Presta, Curr. Op. Struct. Biol. 2:593-596, 1992; U.S. Pat. No. 4,816,567), including techniques such as “superhumanizing” antibodies (Tan et al., J. Immunol. 169: 1119, 2002) and “resurfacing” (e.g., Staelens et al., Mol. Immunol. 43: 1243, 2006; and Roguska et al., Proc. Natl. Acad. Sci USA 91: 969, 1994).

A “humaneered” antibody in the context of this invention refers to an engineered human antibody having a binding specificity of a reference antibody. A “humaneered” antibody for use in this invention has an immunoglobulin molecule that contains minimal sequence derived from a donor immunoglobulin. Typically, an antibody is “humaneered” by joining a DNA sequence encoding a binding specificity determinant (BSD) from the CDR3 region of the heavy chain of the reference antibody to human V_(H) segment sequence and a light chain CDR3 BSD from the reference antibody to a human V_(L) segment sequence. A “BSD” refers to a CDR3-FR4 region, or a portion of this region that mediates binding specificity. A binding specificity determinant therefore can be a CDR3-FR4, a CDR3, a minimal essential binding specificity determinant of a CDR3 (which refers to any region smaller than the CDR3 that confers binding specificity when present in the V region of an antibody), the D segment (with regard to a heavy chain region), or other regions of CDR3-FR4 that confer the binding specificity of a reference antibody. Methods for humaneering are provided in US patent application publication no. 20050255552 and US patent application publication no. 20060134098.

The term “hybrid” when used with reference to portions of a nucleic acid or protein, indicates that the nucleic acid or protein comprises two or more subsequences that are not normally found in the same relationship to each other in nature. For instance, the nucleic acid is typically recombinantly produced, having two or more sequences, e.g., from unrelated genes arranged to make a new functional nucleic acid. Similarly, a hybrid protein refers to two or more subsequences that are not normally found in the same relationship to each other in nature.

The term “recombinant” when used with reference, e.g., to a cell, or nucleic acid, protein, or vector, indicates that the cell, nucleic acid, protein or vector, has been modified by the introduction of a heterologous nucleic acid or protein or the alteration of a native nucleic acid or protein, or that the cell is derived from a cell so modified. Thus, e.g., recombinant cells express genes that are not found within the native (non-recombinant) form of the cell or express native genes that are otherwise abnormally expressed, under expressed or not expressed at all. By the term “recombinant nucleic acid” herein is meant nucleic acid, originally formed in vitro, in general, by the manipulation of nucleic acid, e.g., using polymerases and endonucleases, in a form not normally found in nature. In this manner, operably linkage of different sequences is achieved. Thus an isolated nucleic acid, in a linear form, or an expression vector formed in vitro by ligating DNA molecules that are not normally joined, are both considered recombinant for the purposes of this invention. It is understood that once a recombinant nucleic acid is made and reintroduced into a host cell or organism, it will replicate non-recombinantly, i.e., using the in vivo cellular machinery of the host cell rather than in vitro manipulations; however, such nucleic acids, once produced recombinantly, although subsequently replicated non-recombinantly, are still considered recombinant for the purposes of the invention. Similarly, a “recombinant protein” is a protein made using recombinant techniques, i.e., through the expression of a recombinant nucleic acid as depicted above.

The phrase “specifically (or selectively) binds” to an antibody or “specifically (or selectively) immunoreactive with,” when referring to a protein or peptide, refers to a binding reaction where the antibody binds to the protein of interest. In the context of this invention, the antibody typically binds to PcrV with an affinity of 500 nM or less, and has an affinity of 5000 nM or greater, for other antigens.

The terms “identical” or percent “identity,” in the context of two or more polypeptide (or nucleic acid) sequences, refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues (or nucleotides) that are the same (i.e., about 60% identity, preferably 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or higher identity over a specified region, when compared and aligned for maximum correspondence over a comparison window or designated region) as measured using a BLAST or BLAST 2.0 sequence comparison algorithms with default parameters described below, or by manual alignment and visual inspection (see, e.g., NCBI web site). Such sequences are then said to be “substantially identical.” “Substantially identical” sequences also includes sequences that have deletions and/or additions, as well as those that have substitutions, as well as naturally occurring, e.g., polymorphic or allelic variants, and man-made variants. As described below, the preferred algorithms can account for gaps and the like. Preferably, protein sequence identity exists over a region that is at least about 25 amino acids in length, or more preferably over a region that is 50-100 amino acids in length, or over the length of a protein.

A “comparison window”, as used herein, includes reference to a segment of one of the number of contiguous positions selected from the group consisting typically of from 20 to 600, usually about 50 to about 200, more usually about 100 to about 150 in which a sequence may be compared to a reference sequence of the same number of contiguous positions after the two sequences are optimally aligned. Methods of alignment of sequences for comparison are well-known in the art. Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology (Ausubel et al., eds. 1995 supplement)).

Preferred examples of algorithms that are suitable for determining percent sequence identity and sequence similarity include the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al., Nuc. Acids Res. 25:3389-3402 (1977) and Altschul et al., J. Mol. Biol. 215:403-410 (1990). BLAST and BLAST 2.0 are used, with the parameters described herein, to determine percent sequence identity for the nucleic acids and proteins of the invention. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, an expectation (E) of 10, M=5, N=−4 and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength of 3, and expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff & Henikoff, Proc. Natl. Acad. Sci. USA 89:10915 (1989)) alignments (B) of 50, expectation (E) of 10, M=5, N=−4, and a comparison of both strands.

The terms “isolated,” “purified,” or “biologically pure” refer to material that is substantially or essentially free from components that normally accompany it as found in its native state. Purity and homogeneity are typically determined using analytical chemistry techniques such as polyacrylamide gel electrophoresis or high performance liquid chromatography. A protein that is the predominant species present in a preparation is substantially purified. The term “purified” in some embodiments denotes that a protein gives rise to essentially one band in an electrophoretic gel. Preferably, it means that the protein is at least 85% pure, more preferably at least 95% pure, and most preferably at least 99% pure.

The terms “polypeptide,” “peptide” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues. The terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers, those containing modified residues, and non-naturally occurring amino acid polymer.

The term “amino acid” refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function similarly to the naturally occurring amino acids. Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, γ-carboxyglutamate, and O-phosphoserine Amino acid analogs refers to compounds that have the same basic chemical structure as a naturally occurring amino acid, e.g., an a carbon that is bound to a hydrogen, a carboxyl group, an amino group, and an R group, e.g., homoserine, norleucine, methionine sulfoxide, methionine methyl sulfonium. Such analogs may have modified R groups (e.g., norleucine) or modified peptide backbones, but retain the same basic chemical structure as a naturally occurring amino acid. Amino acid mimetics refers to chemical compounds that have a structure that is different from the general chemical structure of an amino acid, but that functions similarly to a naturally occurring amino acid.

Amino acids may be referred to herein by either their commonly known three letter symbols or by the one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single-letter codes.

“Conservatively modified variants” applies to both amino acid and nucleic acid sequences. With respect to particular nucleic acid sequences, conservatively modified variants refers to those nucleic acids which encode identical or essentially identical amino acid sequences, or where the nucleic acid does not encode an amino acid sequence, to essentially identical or associated, e.g., naturally contiguous, sequences. Because of the degeneracy of the genetic code, a large number of functionally identical nucleic acids encode most proteins. For instance, the codons GCA, GCC, GCG and GCU all encode the amino acid alanine. Thus, at every position where an alanine is specified by a codon, the codon can be altered to another of the corresponding codons described without altering the encoded polypeptide. Such nucleic acid variations are “silent variations,” which are one species of conservatively modified variations. Every nucleic acid sequence herein which encodes a polypeptide also describes silent variations of the nucleic acid. One of skill will recognize that in certain contexts each codon in a nucleic acid (except AUG, which is ordinarily the only codon for methionine, and TGG, which is ordinarily the only codon for tryptophan) can be modified to yield a functionally identical molecule. Accordingly, often silent variations of a nucleic acid which encodes a polypeptide is implicit in a described sequence with respect to the expression product, but not with respect to actual probe sequences.

As to amino acid sequences, one of skill will recognize that individual substitutions, deletions or additions to a nucleic acid, peptide, polypeptide, or protein sequence which alters, adds or deletes a single amino acid or a small percentage of amino acids in the encoded sequence is a “conservatively modified variant” where the alteration results in the substitution of an amino acid with a chemically similar amino acid. Conservative substitution tables and substitution matrices such as BLOSUM providing functionally similar amino acids are well known in the art. Such conservatively modified variants are in addition to and do not exclude polymorphic variants, interspecies homologs, and alleles of the invention. Typical conservative substitutions for one another include: 1) Alanine (A), Glycine (G); 2) Aspartic acid (D), Glutamic acid (E); 3) Asparagine (N), Glutamine (Q); 4) Arginine (R), Lysine (K); 5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); 6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W); 7) Serine (S), Threonine (T); and 8) Cysteine (C), Methionine (M) (see, e.g., Creighton, Proteins (1984)).

I. Introduction

The invention relates to antibodies that bind with high affinity to the PcrV antigen from Pseudomonas aeruginosa and are typically functional antagonists of the Type III secretion system. The antibodies comprise variable regions with a high degree of homology to human germ-line V_(H) and V_(L) sequences. The CDR3 sequences of the heavy and light chains comprise a pair of binding specificity determinants (BSD) from the monoclonal anti-PcrV antibody Mab166 (Frank et al., J. Infectious Dis. 186: 64-73, 2002; and U.S. Pat. No. 6,827,935) and the antibodies of the invention compete with Mab166 for binding to a neutralizing epitope on the PcrV protein (see, e.g., U.S. Pat. No. 6,827,935).

The BSD sequence in CDRH3 has the amino acid sequence NRGDIYYDFTY (SEQ ID NO:38. In some embodiments, an antibody of the invention as a heavy chain CDR3 sequence NRGDIYYDFTYA(M/F)DX (SEQ ID NO:93), where X is I, S, or Q.

The BSD in CDRL3 is FWXTP (where X may be either S or G; SEQ ID NO:39). Complete V-regions are generated in which the BSD forms part of the CDR3 and additional sequences are used to complete the CDR3 and add a FR4 sequence. Typically, the portion of the CDR3 excluding the BSD and the complete FR4 are comprised of human germ-line sequences. In preferred embodiments, the CDR3-FR4 sequence excluding the BSD differs from human germ-line sequences by not more than 2 amino acids on each chain.

The human germline V-segment repertoire consists of 51 heavy chain V-segments, 40 κ light chain V-segments, and 31λ light chain V-segments, making a total of 3,621 germline V-region pairs. In addition, there are stable allelic variants for most of these V-segments, but the contribution of these variants to the structural diversity of the germline repertoire is limited. The sequences of all human germ-line V-segment genes are known and can be accessed in the V-base database (on the worldwide web at vbase.mrc-cpe.cam.ac.uk), provided by the MRC Centre for Protein Engineering, Cambridge, United Kingdom (see, also Chothia et al., 1992, J Mol Biol 227:776-798; Tomlinson et al., 1995, EMBO J 14:4628-4638; Cook et al. (1995) Immunol. Today 16: 237-242 and Williams et al., 1996, J Mol Biol 264:220-232); or the international ImMunoGeneTics database (IMGT). These sequences can be used as reference sources for the human germline segments of the antibodies of the invention.

Antibodies or antibodies fragments as described herein can be expressed in prokaryotic or eukaryotic microbial systems or in the cells of higher eukaryotes such as mammalian cells.

An antibody that is employed in the invention can be in any format. For example, in some embodiments, the antibody can be a complete antibody including a constant region, e.g., a human constant region, or can be a fragment or derivative of a complete antibody, e.g., a Fab, Fab′, F(ab′)₂, scFv, Fv, or a single domain antibody, such as a nanobody or a camelid antibody.

II. Heavy Chains

A heavy chain of an anti-PcrV antibody of the invention comprises a heavy-chain V-region that comprises the following elements:

1) human heavy-chain V-segment sequences comprising FR1-CDR1-FR2-CDR2-FR3

2) a CDRH3 region comprising the amino acid sequence NRGDIYYDFTY (SEQ ID NO:33)

3) a FR4 contributed by a human germ-line J-gene segment.

Examples of V-segment sequences that support binding to PcrV in combination with a CDR3-FR4 segment described above together with a complementary V_(L) region are shown in FIG. 1. The V-segments can be from the human VH1 or VH3 sub-classes. In some embodiments, the V-segment is a human V_(H)3 sub-class segment that has a high degree of amino-acid sequence identity with the germ-line segment VH3-30.3. For example the V-segment differs by not more than fifteen residues from VH3-30.3 and preferably not more than seven residues.

The FR4 sequence of the antibodies of the invention is provided by a human J segment. There are six heavy chain JH-regions numbered 1 through 6. Thus, the FR4 sequences can be provided by a JH1, JH2, JH3, JH4, JH5 or JH6 gene segment. Typically, the FR4 region of an antibody of the invention has at least 90%, often at least 91%, 92%, 93%, 94%, 95% 96%, 97%, 98%, 99%, or 100% identity, to the FR4 region of the human germline J segment that provides the FR4.

In some embodiments, the FR4 sequence is provided by a human germ-line JH3 segment and has a sequence WGQGTMVTVSS (SEQ ID NO:94). In other embodiments, the FR4 is provided by a human germ-line JH6 segment and has the sequence WGQGTTVTVSS (SEQ ID NO:95).

The CDRH3 also comprises sequences that are derived from a human J-segment. Typically, the CDRH3-FR4 sequence excluding the BSD differs by not more than 2 amino acids from a human germ-line J-segment. In typical embodiments, the J-segment sequences in CDRH3 are from the same J-segment used for the FR4 sequences. Thus, in some embodiments, the CDRH3-FR4 region comprises the BSD and a complete human JH3 germ-line gene segment. Exemplary combinations of CDRH3 and FR4 sequences are shown below, in which the BSD is in bold and human germ-line J-segment residues are underlined:

CDR3 (FR4 = JH3)  (SEQ ID NO: 96) NRGDIYYDFTY AFDIWGQGTMVTVSS (FR4 = JH3) (SEQ ID NO: 97) NRGDIYYDFTY AMDIWGQGTMVTVSS (FR4 = JH6) (SEQ ID NO: 98) NRGDIYYDFTYAMDIWGQGTTVTVSS

In some embodiments, an antibody of the invention comprises a V-segment that has at least 90% identity, or at least 91%, 92% 93%, 94%, 95%, 965, 97%, 98%, 99%, or 100% identity to the germ-line segment VH3 30.3 or to a germlineVH1-18 segment; or to one of the V-segments of the V_(H) regions shown in FIG. 1, such as a V-segment portion of SEQ ID NOS:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 26, 27, 29, and 35.

In some embodiments, the V-segment of the VH region has a CDR1 and/or CDR2 as shown in FIG. 1. For example, an antibody of the invention may have a CDR1 that has the sequence TAGMH (SEQ ID NO:50), SYGIH (SEQ ID NO:51), SYGMH (SEQ ID NO:52), SYPLH (SEQ ID NO:53), or NYPMH (SEQ ID NO:54); or a CDR2 that has the sequence VIWYNGKEISYADSVKG (SEQ ID NO:55), FISYDGSEKYYASSVKG (SEQ ID NO:56), or VISYDGSEKWYADSVKG (SEQ ID NO:57). In some embodiments, the CDR2 of the VH region has a negatively charged amino acid positioned in about the middle, e.g., at position 8 or 9 of the CDR2.

In particular embodiments, an antibody has both a CDR1 and a CDR2 from one of the V_(H) region V-segments shown in FIG. 1 and a CDR3 that comprises NRGDIYYDFTY (SEQ ID NO:38), e.g., NRGDIYYDFTYAFDI (SEQ ID NO:63) or NRGDIYYDFTYAMDI (SEQ ID NO:99). Thus, an anti-PcrV antibody of the invention, may for example, have a CDR3-FR4 that has the sequence NRGDIYYDFTYAFDIWGQGTMVTVSS (SEQ ID NO:96), NRGDIYYDFTYAMDIWGQGTMVTVSS (SEQ ID NO:97), or NRGDIYYDFTYAMDIWGQGTTVTVSS (SEQ ID NO:98). In other embodiments, the antibody may comprise a CDR3 that has the sequence NRGDIYYDFTYA(M/F)D(Q/S) (SEQ ID NO:100).

III. Light Chains

A light chain of an anti-PcrV antibody of the invention comprises at light-chain V-region that comprises the following elements:

1) human light-chain V-segment sequences comprising FR1-CDR1-FR2-CDR2-FR3

2) a CDRL3 region comprising the sequence FWXTP (where X may be S or G; SEQ ID NO:39)

3) a FR4 contributed by a human germ-line J-gene segment.

The V_(L) region comprises either a Vlambda or a Vkappa V-segment. Examples of Vlambda and Vkappa sequences that support binding in combination with a complementary V_(H)-region are provided in FIG. 2. Vkappa segments are cloned upstream of the human germ-line JK2 segment and Vlambda segments are cloned upstream of the germ-line JL2 segment.

The CDRL3 sequence comprises a V-segment and J-segment derived sequences. In typical embodiments, the J-segment sequences in CDRL3 are from the same J-segment used for FR4. Thus, may differ by not more than 2 amino acids from human kappa germ-line V-segment and J-segment sequences. In some embodiments, the CDRL3-FR4 region comprises the BSD and the complete human JK2 germ-line gene segment. Exemplary CDRL3-FR4 combinations for kappa chains are shown below in which the BSD is shown in bold and JK2 sequences are underlined:

CDR3 (JK2) (SEQ ID NO: 101) QQFWSTP YTFGQGTKLEIK (JK2) (SEQ ID NO: 102) QHFWGTP YTFGQGTKLEIK

A preferred CDR3-FR4 for lambda chains is shown below in which the BSD is shown in bold and the JL2 sequences are underlined:

CDR3 (JL2) (SEQ ID NO: 103) QHFWSTPYTFGGGTKLTVL

The FR4 sequence of the antibodies of the invention is provided by a human J segment. There are five human JKappa-region segments labeled 1 though 5 and four JLambda-region segments labeled 1, 2, 3 and 7. Thus, the FR4 sequences can be provided by by any of these germline sequences. Typically, the FR4 region of an antibody of the invention has at least 90%, often at least 91%, 92%, 93%, 94%, 95% 96%, 97%, 98%, 99%, or 100% identity, to the FR4 region of the human germline J segment that provides the FR4.

The Vkappa segments are typically of the VKI or VKIII sub-class. In some embodiments, the segments have at least 80% sequence identity to a human germline VKI or VKIII subclass, e.g., at least 80% identity to the human germ-line VKI L12 sequence or to human germline VKIII L2 or VKIII A11 sequence. For example, the Vkappa segment may differ by not more than 18 residues from VKI L12, or 12 residues from VKIII A11 or VKIII L2. In other embodiments, the V_(L) region V-segment of an antibody of the invention has at least 85% identity, or at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identity to the human germline VKI L12, or to the human germline VkIII L2 sequence, or to human germline VKIII A11 sequence, or to a kappa V-segment sequence of a V_(L) region shown in FIG. 2, for example, the V-segment sequence of SEQ ID NOS:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, or 37.

In some embodiments, the V-segment of the V_(L) corresponds to a human germline Vlambda segment. Thus, in some embodiments, the V-segment has at least 85% identity, or at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or 100% identity to a Vlambda V-segment of a V_(L) region of FIG. 2, such as the V-segment sequence of SEQ ID NOS:28, 30, 32, or 34.

In some embodiments, the V-segment of the V_(L) region has a CDR1 and/or CDR2 as shown in FIG. 2. For example, an antibody of the invention may have a CDR1 sequence of RASQGISTYLA (SEQ ID NO:66), RASQGISSWLA (SEQ ID NO:67), RASQSISRWVA (SEQ ID NO:68), or RASEGVDRWLA (SEQ ID NO:69) or CDR2 sequence AASSLQS (SEQ ID NO:70), DASSLKS (SEQ ID NO:71), DASALQS (SEQ ID NO:72), or DASTLQS (SEQ ID NO:73). In other embodiments, the antibody may have a CDR1 sequence of QGDSLRSYYA (SEQ ID NO:104), TGTSSDVGAYNYVS (SEQ ID NO:79), or TGTSSDYV (SEQ ID NO:105); or a CDR2 sequence GKNNRPS (SEQ ID NO:106), EVTKRPS (SEQ ID NO:107), or DVTNRPS (SEQ ID NO:108).

In particular embodiments, an anti-PcrV antibody of the invention may have a CDR1 and a CDR2 in a combination as shown in one of the V-segments of the V_(L) regions set forth in FIG. 2 and a CDR3 sequence that comprises FWXTP (SEQ ID NO:39), where X is S or G, e.g., the CDR3 may be QQFWSTPYT (SEQ ID NO:109), QHFWGTPYT (SEQ ID NO:110), or QHFWSTPYT (SEQ ID NO:111). In some embodiments, such an anti-PcrV antibody may comprise an FR4 region that is FGQGTKLEIK (SEQ ID NO:47) or FGGGTKLTVL (SEQ ID NO:48). Thus, an anti-PcrV antibody of the invention, can comprise, e.g., both the CDR1 and CDR2 from one of the V_(L) regions shown in FIG. 2 and a CDR3-FR4 region that is QQFWSTPYTFGQGTKLEIK (SEQ ID NO:101), QHFWGTPYTFGQGTKLEIK (SEQ ID NO:102), or QHFWSTPYTFGGGTKLTVL (SEQ ID NO:103).

IV. Preparation of PcrV Antibodies

An antibody of the invention may comprise any of the V_(H) regions of SEQ ID NOS:1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 26, 27, 29, or 35 in combination with any of the V_(L) regions of SEQ ID NOS:2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 28, 30, 32, 34, 36 or 37.

An antibody may be tested to confirm that the antibody retains the activity of antagonizing the Type III secretion system. The antagonist activity can be determined using any number of endpoints, including cytotoxicity assays. Exemplary assays are described, e.g., in U.S. Pat. No. 6,827,935. An antibody that is administered to treat P. aeruginosa infection preferably retains at least 75%, preferably 80%, 90%, 95%, or 100%, of the Type III secretion pathway antagonist activity of Mab166 (U.S. Pat. No. 6,827,935).

A high-affinity antibody may be identified using well known assays to determine binding activity and affinity. Such techniques include ELISA assays as well as binding determinations that employ surface plasmon resonance or interferometry. For example, affinities can be determined by biolayer interferometry using a ForteBio (Mountain View, Calif.) Octet biosensor.

Antibodies of the invention typically compete with Mab166 for binding to PcrV. The region of PcrV to which Mab166 binds has been identified (U.S. Pat. No. 6,827,935). PcrV or a fragment thereof that binds Mab 166 can be employed in a competitive binding assay. The ability of an antibody described herein to block or compete with Mab166 for binding to PcrV indicates that the antibody binds to the same epitope as Mab166 or to an epitope that is close to, e.g., overlapping, with the epitope that is bound by Mab166. In other embodiments an antibody described herein, e.g., an antibody comprising a V_(H) and V_(L) region combination as shown in Table 1, can be used as a reference antibody for assessing whether another antibody competes for binding to PcrV. A test antibody is considered to competitively inhibit binding of a reference antibody, if binding of the reference antibody to the antigen is reduced by at least 30%, usually at least about 40%, 50%, 60% or 75%, and often by at least about 90%, in the presence of the test antibody. Many assays can be employed to assess binding, including ELISA, as well as other assays, such as immunoblots.

In some embodiments, the anti-PcrV antibody need not antagonize the Type III secretion sequences. For example, antibodies of the invention that bind to PcrV can recruit multiple cell types of the immune system to stimulate phagocytosis by macrophages, antibody directed cellular cytotoxicity (ADCC) by macrophages or NK cells, activation of the complement cascade, and/or generation of the oxidative burst by neutrophils, thereby causing bacterial, i.e., P. aeruginosa, death. Furthermore, all antibody variable regions are capable of catalyzing redox reactions from singlet oxygen provided by activated neutrophils, leading to the generation of a variety of highly potent oxidizing agents directly harmful to bacteria (see, e.g., Wentworth et al., Proc. Natl. Acad. Sci USA 97:10930-10935, 2000), including ozone, a potent antibacterial agent which also stimulates inflammatory responses (see, e.g., Babior et al., Proc. Natl. Acad. Sci USA 100:3031-3034, 2003). Indeed, inflammation induced by complement activation and ozone generation has the potential to recruit additional elements of the immune system to further boost immunity. Such antibodies typically have an affinity of 50 nM or less, typically less than about 10 nM.

Non-neutralizing and neutralizing anti-PcrV antibodies used in combination with antibiotics provide a strong therapeutic effect.

Methods for the isolation of antibodies with V-region sequences close to human germ-line sequences have previously been described (US patent applications 20050255552 and 20060134098). Antibody libraries may be expressed in a suitable host cell including mammalian cells, yeast cells or prokaryotic cells. For expression in some cell systems, a signal peptide can be introduced at the N-terminus to direct secretion to the extracellular medium. Antibodies may be secreted from bacterial cells such as E. coli with or without a signal peptide. Methods for signal-less secretion of antibody fragments from E. coli are described in US patent application 20070020685.

To generate a PcrV-binding antibody, one of the V_(H)-regions of the invention is combined with one of the V_(L)-regions of the invention and expressed in any of a number of formats in a suitable expression system. Thus the antibody may be expressed as a scFv, Fab, Fab′ (containing an immunoglobulin hinge sequence), F(ab′)₂, (formed by di-sulfide bond formation between the hinge sequences of two Fab′ molecules), whole immunoglobulin or truncated immunoglobulin or as a fusion protein in a prokaryotic or eukaryotic host cell, either inside the host cell or by secretion. A methionine residue may optionally be present at the N-terminus, for example, in polypeptides produced in signal-less expression systems. Each of the V_(H)-regions described herein may be paired with each of the V_(L) regions to generate an anti-PcrV antibody. For example, VH3 1080-2F was identified from the library paired with two different lambda light chains (1080-2F and 1080-11E). The kappa chain 1069-3F was identified paired with VH3 1069-3F and with VH3 1100-3. Exemplary combinations of heavy and light chains are shown in the Table 1.

TABLE 1 Exemplary antibody heavy-chain and light-chain combinations VH Vkappa SEQ ID NO: 1 SEQ ID NO: 2 SEQ ID NO: 11 SEQ ID NO: 12 SEQ ID NO: 3 SEQ ID NO: 12 SEQ ID NO: 7 SEQ ID NO: 8 SEQ ID NO: 9 SEQ ID NO: 10 SEQ ID NO: 5 SEQ ID NO: 6 SEQ ID NO: 13 SEQ ID NO: 37 SEQ ID NO: 21 SEQ ID NO: 18 SEQ ID NO: 17 SEQ ID NO: 18 SEQ ID NO: 26 SEQ ID NO: 24 SEQ ID NO: 25 SEQ ID NO: 24 SEQ ID NO: 23 SEQ ID NO: 24 SEQ ID NO: 29 SEQ ID NO: 20 SEQ ID NO: 35 SEQ ID NO: 36 Vlambda SEQ ID NO: 29 SEQ ID NO: 28 SEQ ID NO: 29 SEQ ID NO: 30 SEQ ID NO: 29 SEQ ID NO: 34 SEQ ID NO: 3 SEQ ID NO: 32

In many embodiments, the antibodies of the invention antagonize the P. aeruginosa type III secretion system and typically exhibit high affinity binding to PcrV. High affinity binding between an antibody and an antigen exists if the affinity of the antibody is less than 500 or 100 nM, for example, less than 50 nM or less than 25 nM, or less than 10 nM, or less than 1 nM, e.g., less than about 100 pM. The antibodies of the invention typically have an affinity of 50 nM or less, often 10 nM or less, when assayed as Fabs, e.g., using ELISA, surface plasmon resonance assays, or interferometry. Table 1 provides examples of such antibodies.

In some embodiments, an antibody of the invention is more potent in a cellular cyototxicity assay than Mab166.

Antibodies may be produced using any number of expression systems, including both prokaryotic and eukaryotic expression systems. Many such systems are widely available from commercial suppliers. In embodiments in which an antibody comprises both a V_(H) and V_(L) region, the V_(H) and V_(L) regions may be expressed using a single vector, e.g., in a discistronic expression unit, or under the control of different promoters. In other embodiments, the V_(H) and V_(L) region may be expressed using separate vectors. The antibodies of the invention may be expressed with or without a methionine at the N-terminus Thus, a V_(H) or V_(L) region as described herein may optionally comprise a methionine at the N-terminus.

An antibody of the invention may be produced in any number of formats, including as a Fab, a Fab′, a F(ab′)₂, a scFv, or a dAB. An antibody of the invention can also include a human constant region. The constant region of the light chain may be a human kappa or lambda constant region. The heavy chain constant region is often a gamma chain constant region, for example, a gamma-1, gamma-2, gamma-3, or gamma-4 constant region. In other embodiments, the antibody may be an IgA.

In some embodiments, the antibody is “non-immunogenic” when administered to a human. The term “non-immunogenic” as used here refers to a PcrV antibody of the invention that does not provoke antibody production against the anti-PcrV antibody when administered to a human. Antibodies can be assessed for immunogenicity using known assays, e.g., an electrochemiluminescence immunoassay described in example 5. Such assays detect the level of antibodies present in a patient, e.g., in a serum sample from the patient, that react with the anti-PcrV antibody that is administered to the patient. An assay is considered to show that the antibody is non-immunogenic when no detectable antibody to the anti-PcrV antibody is present in the sample, e.g., in comparison to a control sample from an individual that was not administered the antibody.

V. PEGylation of Antibodies

In some embodiments, e.g., where the antibody is a fragment, the antibody can be conjugated to another molecule, e.g., polyethylene glycol (PEGylation) or serum albumin, to provide an extended half-life in vivo. Examples of PEGylation of antibody fragments are provided in Knight et al. Platelets 15:409, 2004 (for abciximab); Pedley et al., Br. J. Cancer 70:1126, 1994 (for an anti-CEA antibody); Chapman et al., Nature Biotech. 17:780, 1999; and Humphreys, et al., Protein Eng. Des. 20: 227, 2007).

In some embodiments, the antibodies of the invention are in the form of a Fab′ fragment. A full-length light chain is generated by fusion of a V_(L)-region to human kappa or lambda constant region. Either constant region may be used for any light chain; however, in typical embodiments, a kappa constant region is used in combination with a Vkappa variable region and a lambda constant region is used with a Vlambda variable region.

The heavy chain of the Fab′ is a Fd′ fragment generated by fusion of a V_(H)-region of the invention to human heavy chain constant region sequences, the first constant (CH1) domain and hinge region. The heavy chain constant region sequences can be from any of the immunoglobulin classes, but is often from an IgG, and may be from an IgG1, IgG2, IgG3 or IgG4. The Fab′ antibodies of the invention may also be hybrid sequences, e.g., a hinge sequence may be from one immunoglobulin sub-class and the CH1 domain may be from a different sub-class. In a preferred embodiment, the heavy chain constant region including the CH1 domain and hinge sequence is from human IgG1.

The Fab′ molecule can be PEGylated using known methods. The hinge region of the heavy chain contains cysteine residues suitable for conjugation to a polyethylene glycol derivative. The hinge sequence may be the complete natural hinge region of an immunoglobulin heavy chain or may be truncated by one or more amino-acids. In some embodiments, the hinge region may be a modified or synthetic sequence. In further embodiments, the hinge is a natural immunoglobulin hinge sequence and contains two cysteine residues.

In some embodiments, Fab′ molecules can be conjugated by site-specific conjugation to maleimide derivatives of methoxy polyethylene glycol (mPEG-mal). The mPEG-mal can have, for example, an average molecular mass of between 10 and 40 kD. The PEG may be branched PEG or linear PEG. In some embodiments, the mPEG-mal is a linear molecule and has an approximate molecular weight of 30 kD. One or more molecules of mPEG-mal is conjugated to each Fab′ molecule. The mPEG molecules are conjugated via thioether linkages between the maleimide moiety of mPEG-mal and one or more of the cysteine residues in the hinge region of the Fab′ heavy chain to form the PEGylated Fab′ molecule. The mPEG-mal is conjugated in suitable buffer and under conditions suitable for thioether formation using methods known in the art for conjugation of maleimide derivatives to thiol-groups on proteins.

The Fab′ may be produced from the expression system in a form in which the hinge cysteine groups are in an oxidized form. In this case, the Fab′ may be subjected to a reduction step prior to conjugation. Reducing agents suitable for generation of free hinge thiols and methods for selective reduction of hinge cysteines are known in the art and include the use of dithiothreitol (DTT), beta-mercapto-ethanol, beta-mercapto-ethylamine (MEA) and non-thiol reducing agents such as tris(2-carboxyethyl) phosphine. In some embodiments, the reduction is carried out under conditions such that the hinge cysteines are selectively reduced and PEGylation occurs predominantly at the hinge. Typically, the PEGylated Fab′ comprises two molecules of mPEG due to PEGylation of both cysteine residues in the hinge. In some embodiments, a mutation may be introduced into the hinge region to replace one of the cysteine residues with another amino acid. Derivatization of such a mutant with mPEG-mal leads to the generation of mono-PEGylated Fab′.

Examples of suitable sequences of hinges are:

natural human gamma-1 hinge for di-PEGylation (SEQ ID NO: 112) THTCPPCPA Mutant Hinge-1 for mono-PEGylation (SEQ ID NO: 113) THTAPPCPA Mutant Hinge-2 for mono-PEGylation (SEQ ID NO: 114) THTCPPAPA

Other methods of PEGylation, for example, where the PEG is not introduced at a hinge are also known. For example, Humphreys et al., supra, describe methods for PEGylation of cysteine residues outside the hinge region by disruption of the interchain disulphide bond between the heavy and light chain of a Fab.

Methods for purification of PEGylated Fab′ and separation of the desired mono- or di-PEGylated Fab′ from unreacted mPEG-maleimide and Fab′ molecules containing higher numbers of PEG moieties are known in the art. Such methods include, for example, size-exclusion or ion-exchange chromatography.

VI. Administration of PcrV Antibodies for the Treatment of P. aeruginosa Infections.

The invention also provides methods of treating a patient that has, or is at risk of having, a P. aeruginosa infection by administering an antibody of the invention. In some embodiments, such a patient has cystic fibrosis, ventilator-associated pneumonia (VAP), cancer-associated neutropenia, or burns. The methods of the invention comprise administering a PcrV antibody as a pharmaceutical composition to an P. aeruginosa-infected patient in a therapeutically effective amount using a dosing regimen suitable for treatment of the disease. The composition can be formulated for use in a variety of drug delivery systems. One or more physiologically acceptable excipients or carriers can also be included in the compositions for proper formulation. Suitable formulations for use in the present invention are found in Remington's Pharmaceutical Sciences, Mack Publishing Company, Philadelphia, Pa., 17th ed. (1985). For a brief review of methods for drug delivery, see, Langer, Science 249: 1527-1533 (1990).

The PcrV antibody is provided in a solution suitable for injection into the patient such as a sterile isotonic aqueous solution for injection. The antibody is dissolved or suspended at a suitable concentration in an acceptable carrier. In some embodiments the carrier is aqueous, e.g., water, saline, phosphate buffered saline, and the like. The compositions may contain auxiliary pharmaceutical substances as required to approximate physiological conditions, such as pH adjusting and buffering agents, tonicity adjusting agents, and the like.

The pharmaceutical compositions of the invention are administered to a patient, e.g., a cystic fibrosis patient having a P. aeruginosa infection, in an amount sufficient to cure or at least partially arrest the disease or symptoms of the disease and its complications. An amount adequate to accomplish this is defined as a “therapeutically effective dose.” A therapeutically effective dose is determined by monitoring a patient's response to therapy. Typical benchmarks indicative of a therapeutically effective dose include amelioration of symptoms of infection in the patient, or a decrease in the levels of P. aeruginosa in the patient. Amounts effective for this use will depend upon the severity of the disease and the general state of the patient's health, including other factors such as age, weight, gender, administration route, etc. Single or multiple administrations of the antibody may be administered depending on the dosage and frequency as required and tolerated by the patient. In any event, the methods provide a sufficient quantity of PcrV antibody to effectively treat the patient.

The antibody may be administered alone, or in combination with other therapies to treat the P. aeruginosa infection

The antibody can be administered by injection or infusion through any suitable route including but not limited to intravenous, sub-cutaneous, intramuscular or intraperitoneal routes. In some embodiments, the antibody may be administered by insufflation. In an exemplary embodiment, the antibody may be stored at 10 mg/ml in sterile isotonic aqueous saline solution for injection at 4° C. and is diluted in either 100 ml or 200 ml 0.9% sodium chloride for injection prior to administration to the patient. The antibody is administered by intravenous infusion over the course of 1 hour at a dose of between 0.2 and 10 mg/kg. In other embodiments, the antibody is administered by intravenous infusion over a period of between 15 minutes and 2 hours. In still other embodiments, the administration procedure is via sub-cutaneous bolus injection.

The dose of antibody is chosen in order to provide effective therapy for the patient and is in the range of less than 0.1 mg/kg body weight to 25 mg/kg body weight or in the range 1 mg-2 g per patient. Preferably the dose is in the range 1-10 mg/kg or approximately 50 mg-1000 mg/patient. The dose may be repeated at an appropriate frequency which may be in the range once per day to once every three months, depending on the pharmacokinetics of the antibody (e.g. half-life of the antibody in the circulation) and the pharmacodynamic response (e.g. the duration of the therapeutic effect of the antibody). In some embodiments, the in vivo half-life of between about 7 and about 25 days and antibody dosing is repeated between once per week and once every 3 months. In other embodiments, the antibody is administered approximately once per month.

In further embodiments, the antibody is PEGylated. For example, an antibody of the invention may be PEGylated, e.g., using methods as described herein, and administered to a patient infected with P. aeruginosa.

A V_(H) region and/or V_(L) region of the invention may also be used for diagnostic purposes. For example, the V_(H) or V_(L) region may be used for clinical analysis, such as detection of P. aeruginosa in samples from patient that have, or are suspected of having, a P. aeruginosa infection. A V_(H) or V_(L) region of the invention may also be used, e.g., to produce anti-Id antibodies.

EXAMPLES Example 1 Identification of Engineered Human Anti-PcrV Fab Molecules

Epitope-focused engineered human antibody Fab libraries were generated as described in US patent application 20050255552. V-segment sequences derived from repertoires of human immunoglobulin sequences were cloned upstream of a selected CDR3-FR4 sequence for each of the heavy and light chains.

For heavy-chain repertoires, the CDRH3 comprises a D-segment derived sequence (NRGDIYYDFTY; SEQ ID NO:38) from a previously identified anti-PcrV monoclonal antibody (Mab 166; Frank et al 2002 J. Infectious Dis. 186: 64-73) which constitutes a binding specificity determinant. The sequence of the complete CDRH3-FR4 sequence for the heavy chain repertoires is shown below.

For VH1 library 1015, the CDR3-FR4 combination used was:

CDR3 (FR4 = JH3) (SEQ ID NO: 96) NRGDIYYDFTY AFDIWGQGTMVTVSS For VH3 libraries, the CDR3-FR4 combination used differed by a single amino acid in

CDRH3:

CDR3 (FR4 = JH3) (SEQ ID NO: 97) NRGDIYYDFTY AMDIWGQGTMVTVSS

For light-chain repertoires, human Vkappa or Vlambda sequences comprising FR1-CDRL1-FR2-CDRL2-FR3 were inserted upstream of selected CDRL3-FR4 sequences. The CDRL3 comprises a binding specificity determinant from Mab 166 light-chain with the sequence FWXTP (where X may be S or G; SEQ ID NO:39). For Vkappa libraries, the C-terminal residues of CDRL3 and FR4 were contributed by the human germ-line JK2 sequence YTFGQGTKLEIK (SEQ ID NO:115; JK2 residues within CDRL3 are underlined). For Vlambda libraries, the FR4 region was contributed by JL2 germ-line sequence FGGGTKLTVL (SEQ ID NO:48). The JL2 germline sequence is identical to the JL3 sequence.

In some cases cassette libraries were constructed as described in US patent application 20060134098 (library 1070). For library 1080, full-length lambda chains were screened in combination with VH cassette libraries.

Heavy and light chain polypeptides were expressed as mature proteins, i.e., without a signal peptide, and secreted in E. coli cells that express a mutant SecY gene as described in US patent application 20070020685. The peptides therefore were expressed with an N-terminal methionine. Binding of recombinant Fabs to PcrV was identified by a filter-binding assay using nitrocellulose filters coated with GST-PcrV fusion protein as described in US patent application 20050255552. Binding activity was confirmed by antigen ELISA using plates coated with GST-PcrV and affinities were determined by biolayer interferometry using a ForteBio Octet biosensor.

The sequences of the V-regions of exemplary high-affinity anti-PcrV antibodies are shown in FIG. 1 and FIG. 2.

Each of the Fabs has high affinity for PcrV. Several Fabs were identified with affinities at least equivalent to Mab166 Fab (approximately 1.4 nM) determined by biolayer interferometry using a ForteBio (Mountain View, Calif.) Octet biosensor.

VH and VL regions identified as described can be used in various combinations. For example, a V_(K) light chain SEQ ID NO:12 supports high affinity binding to PcrV in combination with either a V_(H) comprising SEQ ID NO:11, or a V_(H) comprising SEQ ID NO:3.

The 1070-9E antibody is an example of a high affinity antibody derived by V-region cassette exchange using methods described in US Patent Application Publication NO. 20060134098. To isolate this antibody, 4 V-region replacement cassettes were constructed: 1) heavy chain front-end cassette (consisting of human VH3 FR1-CDR1-FR2 sequences) 2) heavy chain middle cassette (consisting of human VH3 FR2-CDR2-FR3 sequences) 1) light chain front-end cassette (consisting of human VK1 FR1-CDR1-FR2 sequences) 2) light chain middle cassette (consisting of human VK1 FR2-CDR2-FR3 sequences). Each cassette was assembled with additional V-region sequences from Mab 166 and the selected CDR3-FR4 region and expressed as Fab fragments in E. coli TOP10 cells transformed with a plasmid over-expresssing a mutant SecY gene to allow secretion of signal-less Fabs. Cassette Fab libraries were then screened on GST-PcrV coated filters to identify PcrV binders. Selected sequences from Fabs supporting PcrV binding were then recombined and re-screened to identify fully-human V-segments supporting high-affinity binding to PcrV.

Fab 1070-9E, isolated by cassette recombination, has an affinity for recombinant PcrV of 1.48 nM, determined by biolayer interferometry.

High-affinity anti-PcrV Fabs are also potent antagonists of the P. aeruginosa Type III Secretion system and inhibit P. aeruginosa exotoxin-mediated killing of P3-X63 Ag8 myeloma cells by P. aeruginosa strain PA103 in a cell-based cytotoxicity assay.

Example 2 PEGylated Fab′

In this example, a Fab′ consisting of a human Fd′ heavy chain of the IgG1 sub-class and human kappa light chain linked by an inter-chain disulfide bond involving the C-terminal cysteine of the kappa chain and the cysteine residue C227 of the heavy chain (numbering sequentially from the N-terminus of the mature protein) was PEGylated. The recombinant Fd′ heavy chain contains the IgG1 CH1 domain and the IgG1 hinge region including two cysteine residues which are available after reduction for conjugation to maleimide groups. Thus the expressed antibody protein is a disulfide-linked heterodimer of Fd′ heavy chain and a kappa light chain, containing a total of 452 amino acids. The sequence of the constant region of an exemplary Fd′ is shown in FIG. 3.

To generate an immunoconjugate with a reduced rate of in vivo clearance and thus an improved pharmacokinetic profile, the Fab′ is conjugated to polyethylene glycol (PEG). In di-PEGylated Fab′, each molecule of Fab′ is conjugated to two long-chain PEG molecules by site-specific attachment at the hinge region exploiting the two available reactive thiols on the hinge cysteine residues and a maleimide derivatized PEG, methoxy-polyethylene glycol maleimide (mPEG-mal). The mPEG-mal molecules are conjugated via thioether linkages between the maleimide moiety and the hinge cysteine residues.

To generate di-PEGylated Fab′, mPEG-mal with average molecular weight of 30 kD was obtained from NOF Corporation. The Fab′, which was expressed and secreted from E. coli, was prepared at a concentration of 4 mg/ml in sodium citrate buffer pH 6.5 with 2 mM EDTA. Reducing agent (10 mM MEA at pH 6.5) was added for 30 minutes at room temperature and the reaction mixture was immediately desalted using a Zeba Desalt column (Pierce) pre-equilibrated with 10 mM glycine (pH 3) and 2 mM EDTA. mPEG-mal was added for 1 hour at room temperature and di-PEGylated Fab′ was separated from other PEGylated species and from unreacted Fab′ using a HiTrap SP sepharose column on an Akta purification system from GE Healthcare.

The structure of di-PEGylated Fab′ is provided schematically in FIG. 4. The exemplary di-PEGylated Fab′ PEGylated in this example binds with high affinity to PcrV (affinity of 0.6 nM determined by surface plasmon resonance analysis) and is a potent antagonist of the P. aeruginosa Type III Secretion System.

Mono-PEGylated Fab′ can be generated using mutant derivatives of Fab′ containing only a single hinge cysteine. The sequences of the mutant hinges are:

Wild-type human gamma-1 hinge (SEQ ID NO: 112) THTCPPCPA  Mutant Hinge-1 (SEQ ID NO: 113) THTAPPCPA  Mutant Hinge-2 (SEQ ID NO: 114) THTCPPAPA 

Example 3 Cytotoxicity Assay for Detection of Antibodies and Fab Fragments with Potent Neutralization Activity Against the P. aeruginosa Type III Secretion System

A TTSS-dependent cytotoxicity assay was established using P3-X63-Ag8 (X63) mouse myeloma cells (ATCC) as the target. Cells were cultured in RPMI 1640 (Media Tech) with 10% FBS (Hyclone). About 10⁵ cells were infected with P. aeruginosa strain PA103 at a multiplicity of infection (MOI) of 10 in a volume of 0.1 ml culture medium in wells of a 96-well plate in the presence of Fab. Prior to addition of Fab and mammalian cells, PA 103 was grown in MinS medium (Hauser A R et al. (1998) Infect Immun. 66:1413-1420) to induce expression of the TTSS. After incubation for three hours at 37° C. with 5% CO2, with various concentrations of anti-PcrV Fab, cells were transferred to 12×75 mm flow-cytometry tubes and stained with propidium iodide (Sigma) according to the manufacturer's instructions. The proportion of permeabilized cells was quantified by flow cytometry using a FACS Caliber flow cytometer. Data were analyzed using Prism4 software (Graphpad). (Cytotoxicity was normalized to dead cells in untreated samples). For comparison of the potency of different Fabs, mean concentrations required for 50% inhibition (IC₅₀) were obtained from at least 3 independent assays. Results for several exemplary Fabs are shown in Table 2 below.

TABLE 2 Potency of Fabs in cytotoxicity assay Fab IC₅₀ (nM) Mab166 Fab 53.0 SEQ ID NOS: 13, 4 20.0 SEQ ID NOS: 13, 37 12.0 SEQ ID NOS: 5, 6 50.2 SEQ ID NOS: 13, 10 25.5 SEQ ID NOS: 3, 4 35.1 SEQ ID NOS: 24, 26 25.5 SEQ ID NOS: 35, 36 61.4

Each of the Fabs tested shows potent neutralization of the TTSS and protection of mammalian cells from cytotoxicity.

Several Fabs are more potent in this assay than Mab 166 Fab. Thus, anti-PcrV antibodies of the invention typically show enhanced potency relative to Mab 166 Fab.

Example 4 Effects of an Antibody of the Invention In Vivo Using a Mouse Model of Pneumonia

Experiments were performed in vivo using humaneered Fabs to evaluate the effects of the antibodies in a mouse model of pneumonia. Fab 1A8 has a human VH3 sub-class heavy chain, containing the first constant domain of human IgG1, and a human VKI sub-class kappa light chain. The affinity of Fab 1A8 as determined by Biacore is 0.6 nM. Fab 1A8 binds to PcrV with approximately two-fold higher affinity than Mab 166 Fab.

An acute lethality model of Pseudomonas pneumonia was used to assess the in vivo efficacy of Fab 1A8 in comparison with Mab 166. P. aeruginosa strain PA103 was instilled directly into the lungs of mice at a dose of 1.5×10⁶ cfu/mouse by intratracheal administration, an inoculum shown previously to be sufficient to lead to lethality in 100% of the animals (3×LD₉₀) (Sawa et al., Nat Med. 5:392-8, 1999). Survival and body temperature were monitored for 48 hours and surviving mice at this time point were sacrificed for determination of bacterial counts in the lungs. The survival data (FIG. 5) indicated that both the human Fab 1A8 and the murine Fab can prevent lethality caused by the highly cytotoxic PA103 strain. Control mice infected with PA103 and treated with an irrelevant control Fab, were all dead within 24 hours of inoculation. Treatment of mice with 10 μg Mab 166 or Fab 1A8 led to the survival of 100% of the mice at 48 hours. Since Fab 1A8 lacks the antibody Fc-region, antibody effector functions are not required for prevention of lethality. Fab 1A8 was significantly more potent than Mab166 Fab in prevention of lethality. Fab 1A8 provided significant protection from lethality at doses of 1.25 μg and 0.625 μg/mouse, doses at which mouse Mab166 Fab-treated animals showed 100% mortality (P<0.05 for differences between Fab 1A8 and Mab 166 Fab at 2.5 μg, 1.25 μg and 0.625 μg doses). The activity of Fab 1A8 is comparable to that of Mab166 IgG in prevention of lethality.

Fab 1A8 is also effective in inducing recovery of body temperature, indicative of protection from sepsis (FIG. 6). Untreated mice infected with PA103 show a rapid drop in body temperature within the first few hours of infection. Recovery of body temperature within 12-24 hours in the antibody-treated groups correlates with subsequent survival. Doses as low as 1.25 μg/mouse of Fab 1A8 or Mab 166 led to rapid recovery of body temperature and prevented lethality in at least 80% of mice. However, this dose of mouse Mab 166 Fab fragment was insufficient to allow body temperature recovery and all mice in this group were dead at 48 hours post-infection.

Surviving mice at 48 hours post-challenge were also analyzed for the presence of residual Pseudomonas in the lungs. Remarkably, both Mab 166 and the Fab 1A8 fragments analyzed stimulated significant clearance of bacteria (FIG. 7). After 48 hours, the bacterial counts were reduced at least 1000-fold from the infectious dose of 1.5×10⁶ cfu/mouse in all mice treated with 10 μg Fab 1A8. 80% of mice treated with this dose of Fab 1A8 showed no detectable Pseudomonas in the lungs after 48 hours. Higher residual bacterial counts were detected in mice treated with mouse Mab 166 Fab. Human Fab 1A8 has comparable potency to the whole IgG Mab 166 in this analysis indicating that Fc-effector functions do not contribute significantly to the ability of the antibody to stimulate bacterial clearance

A second humaneered Fab that has the Mab 166 minimal essential binding specificity determinant was also evaluated in vivo using a mouse model of pneumonia. Female Balb/c mice (approximately 20 g in weight; Charles River) were inoculated with 1×10⁶ P. aeruginosa strain PA103 by intra-tracheal administration. Prior to inoculation, PA103 bacteria were grown overnight in YPT broth at 37° C., diluted 1:5 in fresh medium and grown for two hours at 37° C. until they reached exponential phase. The culture was centrifuged at room temperature for ten minutes at 2000×g and the pellet resuspended in ˜8 mL phosphate buffered saline (PBS). Bacteria were quantified by absorbance at 600 nm and bacterial colony-forming units verified by colony growth on tryptic soy (TS) agar plates (Teknova, Half Moon Bay, Calif.). Antibody Fab 2 fragment was premixed with bacteria immediately prior to intratracheal instillation. Infected mice were monitored for body temperature (rectal temperatures) and survival for 48 hours.

Control mice treated only with saline solution showed 100% mortality within 24 hours of bacterial inoculation. Mice treated with 10 μg Fab 2 showed complete protection from lethality; 100% of the Fab-treated mice survived at 48 hours.

This example thus shows that humaneered antibodies of the invention exhibit potent in vivo activity against P. aeruginosa. The Fabs are more potent than a parent M166 Fab in vivo.

Example 5 Evaluation of a Humaneered Fab for Immunogenicity in Human

A humaneered antibody PEGylated Fab′ fragment was evaluated for safety, immunogenicity and plasma/serum half-life in human subjects. Subjects received one dose by intravenous (i.v.) injection at 1, 3, or 10 mg/kg.

The humaneered antibody was well tolerated at all dose levels. The concentration of drug in the plasma was measured by ELISA using the PcrV antigen immobilized onto a microtiter plate. GST-PcrV was immobilized onto a microtiter plate overnight at 4° C. The plate was washed and all unadsorbed sites blocked with the addition of block/diluent buffer for at least 60 minutes. After washing the plate, analytes were dispensed onto the pre-coated microtiter plate and incubated for at least 60 minutes. The plate was washed and a solution containing a biotinylated antibody specific to the humaneered Fab was added for 45 minutes. The plate was washed and a HRP-conjugate solution added for 30 minutes. After the final wash step, a tetramethylbenzidine (TMB) peroxidase substrate solution was added and incubated for approximately 6 minutes. The reaction was stopped with a phosphoric acid solution. Color develops in proportion to the amount of pegylated Fab present. Plates were read on a plate reader using two filters (450 nm for detection and 620 nm for background). Concentrations were determined on a standard curve obtained by plotting optical density (OD) versus concentration. The calibration curve was generated using a four-parameter logistic fit. The range for this method in human serum is from 0.200 to 12.8 ng/mL in 1% serum (20.0 ng/mL to 1280 ng/mL in 100% serum).

Pharmacokinetic Profile of Humaneered Antibody in Human Subjects PK 1.0 mg/kg 3.0 mg/kg 10.0 mg/kg Parameter Units n Cohort 1 Cohort 2 Cohort 3 AUC(0-t) ng*hr/mL 4 10440826 (1137824) 33973664 (2930669) 120424224 (17896301) AUC(0-∞) ng*hr/mL 4 10737696 (1235316) 34856666 (3216244) 124429066 (19035293) % Extrap (%) 4 2.72 (0.886) 2.49 (0.935) 3.17 (0.461) Cmax (ng/mL) 4 29334 (2039) 93533 (10738) 347287 (64571) T½ (hr) 4 341 (38.5) 310 (37.9) 338 (14.1) CL (L/hr) 4 0.00693 (0.000823) 0.00556 (0.000573) 0.00473 (0.00112) Vz (L) 4 3.44 (0.730) 2.50 (0.504) 2.31 (0.588)

The humaneered antibody had a terminal plasma half-life of approximately 14 days.

The presence of anti-drug antibodies, i.e., antibodies generated to the humaneered antibody, was tested at: pre-infusion, day 8, day 15 day 29 and day 70 post infusion. Anti-drug antibodies were measured using an electrochemiluminescent assay (ECLA). Positive controls and negative control serum were diluted 1:25 with diluent buffer. The controls were further diluted 1:2 by the addition of an equal volume of 0.8% acetic acid (resulting in 2× solutions) and then incubated at ambient temperature for approximately 15 minutes. Samples were then diluted an additional 1:2 with Label Master Mix (Antibody-Biotin and Antibody-SulfoTag at 0.5 μg/mL final working concentrations) resulting in a final 1:100 dilution. All controls were then incubated for one hour at room temperature with gentle shaking. The Streptavidin-coated standard MA2400 96-well microtiter plate was blocked by adding diluent buffer for 60 minutes. Diluent buffer was removed from plate wells by aspiration and controls were added to the plate and incubated for 60 minutes. The plate was aspirated and washed, and 1× MesoScaleDiscovery® (MSD) Read Buffer T with surfactant was added. The plates were read on an MSD electrochemiluminescence detector within 1 minute. Intensity of relative light units (RLU) produced are in proportion to the amount of anti-drug antibody present

No anti-drug antibodies were detected at any time point. This example thus demonstrates that there was no detectable immunogenicity of the humaneered antibody in humans.

The following provides an exemplary listing of anti-PcrV antibody V-regions of the invention:

Exemplary Anti-PcrV V-regions Vh (VH1) SEQ ID NO: 1  EIQLVQSGAEVKKPGASVKVSCKASGYTFTDHAISWVRQAPGQGLEWMGWISPYSGNPN YAQSLQGRVSLTTDRSTRTAYMELRSLKSDDTAVYYCARNRGDIYYDFTYAFDIWGQGT MVTVSS VkI SEQ ID NO: 2  DIQMTQSPSSVSASVGDRVTITCRASQGISSWLAWYQQKPGRAPKLLIYAASSLQSGVP SRFSGSGSGTGFTLTISSLQPEDVATYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 3  QVQLVESGGGVVQPGGSLRLSCAASGFTFSTAGMHWVRQAPGKGLEWVAVIWYNGKEIS YADSVKGRFTVSRDNPKNTLYLQMSSLRTEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkI SEQ ID NO: 4  DIQMTQSPSSLSASVGDRVTITCRASQSISRWVAWYQQRPGKAPNLLIYDASSLKSGVP SRFSGSGSGTEFTLTISSLQPEDIATYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 5  QVQLVESGGGVVQPGRSLRLSCTASGFSFSSYGMHWVRQAPGKGLEWVAVIWYNGKEIS YADSVKGRFTVSRDNPKNTLYLQMSSLRTEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkI SEQ ID NO: 6  AIQLTQSPSFLSASVGDRVTITCRASQGISTYLAWYQQKPGKAPKLLIYAASSLQSGVP SRFSGSGSGTDFTLTISSLQPEDVATYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 7  QVQLVESGGGLVQPGRSLRLSCVGSGFTFSSYGIHWVRQAPGKGLEWVAVIWYNGKEIS YADSVKGRFTVSRDNLKNTLYLQMSSLRTEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkI SEQ ID NO: 8  DIQMTQSPSFLSASVGDRVTITCRASQGISTYLAWYQQKRGKAPKLLISAASSLQSGVP SRFSGSVSGTDFTLTISSLQSEDFAVYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 9  QVQLVESGGGLVQPGRSLRLSCVGSGFTFSSYGIHWVRQAPGKGLEWVAVIWYNGKEIS YADSVKGRFTVSRDNPKNTLYLQMSSLRTEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkI SEQ ID NO: 10  DIQLTQSPSFLSASVGDRVTITCRASQGISTYLAWYQQKPGKAPKLLIYDASALQSGVP SRFSGSGSGTEFTLTISSLQPEDVATYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 11  EVQLVESGGGVVQPGGSLRLSCAASGFTFSTAGMHWVRQAPGKGLEWVAVIWYNGKEIS YADSVKGRFTVFRDNPKNTLYLQMSSLRTEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkI SEQ ID NO: 12  DIQMTQSPSSLSASVGDRVTITCRASQSISRWVAWYQQRPGKAPNLLIYDASSLKSGVP SRFSGSGSGTEFTLTISSLQPEDIATYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 13  QVQLVESGGGVVQPGRSLRLSCAASGFTFSSYPLHWVRQAPGKGLEWVSFISYDGSEKY YASSVKGRFTISRDNSENTLYLQMNSLRPEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS Vk SEQ ID NO: 14  DIQLTQSPSFLSASVGDRVTITCRASQGISTYLAWYQQKPGKAPKLLIYDASALQSGVP SRFSGSGSGTEFTLTISSLQPEDVATYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 15  EVQLVESGGGVVQPGRSLRLSCTASGFSFSSYGMHWVRQAPGKGLEWVAVIWYDGRNKY YADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkIII SEQ ID NO: 16  EIVLTQFPGTLSLSPGERATLSCRASQNVGSAYLAWYQQKPGQAPRLLIYGASRRAPGI PDRFSGSGSGTDFTLTINRLEPEDFAVYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 17  EVQLVESGGGVVQPGRSLRLSCAASGFTFSSYGMHWVRQAPGKGLEWVAVIWYDGYNKD YADSVKGRFTISRDNSKNTLYLQINSLRAEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkIII SEQ ID NO: 18  EIVMTQSPATLSVSPGERATLSCRASQSVSSNLAWYQQKPGQAPRLLIYGASTRATGIP ARFSGSGSGTEFTLTISSLQSEDFAVYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 19  EVQLVESGGGVVQPGRSLRLSCAASGFTFSSYPLHWVRQAPGKGLEWVSFISYDGSEKY YASSVKGRFTISRDNSENTLYLQMNSLRPEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkIII SEQ ID NO: 20  EIVMTQSPATLSVSPGERATLSCRASQSVSSNLAWYQQKPGQAPRLLFYAASTRATGIP ARFSGSGSGTEFTLTISSLQSEDFAVYYCQQFWSTPYTFGQGTKLEIK Vh SEQ ID NO: 21  EVQLVESGGGLVQPGRSLRLSCVGSGFTFSSYGIHWVRQAPGKGLEWVANIWYDGSSES YIDSVKGRFTVSRDDSRNTVYLQMNSLRPEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS VkIII SEQ ID NO: 22  EIVMTQSPATLSVSPGERATLSCRASQSVSSNLAWYQQKPGQAPRLLIYGASTRATGIP ARFSGSGSGTEFTLTISSLQSEDFAVYYCQQFWSTPYTFGQGTKLEIK VH SEQ ID NO: 23  EVQLVESGGGVVQPGRSLRLSCAASGFTFSNYPMHWVRQAPGKGLEWVAVISYDGSEKW YADSVKGRFTISRDNSKNTLYLEMNSLRPEDTAVYYCARNRGDIYYDFTYAMDQWGQGT TVTVSS Vk SEQ ID NO: 24  DIQLTQSPSTLSASVGDSVTITCRASEGVDRWLAWYQQKPGRAPKLLIYDASTLQSGVP SRFSGSGSGTEFSLTISSLQPDDVATYYCQHFWGTPYTFGQGTKLEIK VH SEQ ID NO: 25  EVQLVESGGGVVQPGRSLRLSCAASGFTFSNYPMHWVRQAPGKGLEWVAVISYDGSEKW YADSVKGRFTISRDNSKNTLYLEMNSLRPEDTAVYYCARNRGDIYYDFTYAMDSWGQGT TVTVSS VH SEQ ID NO: 26  EVQLVESGGGVVQPGRSLRLSCAASGFTFSNYPMHWVRQAPGKGLEWVAVISYDGSEKW YADSVKGRFTISRDNSKNTLYLEMNSLRPEDTAVYYCARNRGDIYYDFTYAMDIWGQGT TVTVSS VH SEQ ID NO: 35  EVQLVESGGGVVQPGRSLRLSCAASGFTFSNYPMHWVRQAPGKGLEWVAVISYDGSEKW YADSVKGRFTISRDNSKNTLYLEMNSLRPEDTAVYYCARNRGDIYYDFTYAMDYWGQGT TVTVSS Vk SEQ ID NO: 36  DIQLTQSPSTLSASVGDSVTITCRASEGVDRWLAWYQQKPGRAPKLLIYDASTLQSGVP SRFSGSGSGTEFSLTISSLQPDDVATYYCQHFWSTPYTFGQGTKLEIK V-regions of Exemplary Antibodies with Lambda light chain Vh SEQ ID NO: 27  EVQLVESGGGVVQPGRSLRLSCAASGFTFSSYPLHWVRQAPGKGLEWVSFISYDGSEKY YASSVKGRFTISRDNSENTLYLQMNSLRPEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS Vl SEQ ID NO: 28  QSALTQPASVSGSPGQSITISCTGTSSDYVSWYQQHPGKAPKLIIYDVTNRPSGVPDRF SGSKSGNTASLTISGLQAEDEADYYCQHFWSTPYTFGGGTKLTVL Vh SEQ ID NO: 29  EVQLVESGGGVVQPGRSLRLSCAASGFTFSSYPLHWVRQAPGKGLEWVSFISYDGSEKY YASSVKGRFTISRDNSENTLYLQMNSLRPEDTAVYYCARNRGDIYYDFTYAMDIWGQGT MVTVSS Vl SEQ ID NO: 30  SSELTQDPAVSVALGQTVRITCQGDSLRSYYASWYQQKPGQAPVLVIYGKNNRPSGIPD RFSGSSSGNTASLTITGAQAEDEADYYCQHFWSTPYTFGGGTKLTVL Additional V_(L) regions: Vl SEQ ID NO: 32  SSELTQDPAVSVALGQTVTITCQGDSLRSLYASWYQQKPGQAPVLVLYSKNSRPSGIPD RFSGSSSGNTASLTITGARAEDEADYYCQHFWSTPYTFGGGTKLTVL Vl SEQ ID NO: 34  QSVLTQPPSASGSPGQSVTISCTGTSSDVGAYNYVSWYQQYPGKVPKLIIYEVTKRPSG VPDRFSGSKSGNTASLTVSGLRAEDEADYYCQHFWSTPYTFGGGTKLTVL VkI SEQ ID NO: 37  DIQMTQSPSSLSASVGDRVTITCRASQSISRWVAWYQQRPGKAPNLLIYDASSLKSGVP SRFSGSGSGTEFTLTISSLQPEDIATYYCQQFWGTPYTFGQGTKLEIK

Although the foregoing invention has been described in some detail by way of illustration and example for purposes of clarity of understanding, it will be readily apparent to one of ordinary skill in the art in light of the teachings of this invention that certain changes and modifications may be made thereto without departing from the spirit or scope of the appended claims.

All publications, accession numbers, patents, and patent applications cited in this specification are herein incorporated by reference as if each was specifically and individually indicated to be incorporated by reference. 

What is claimed is:
 1. An isolated anti-PcrV antibody that selectively binds PcrV, wherein the antibody comprises a V_(L) region that has a CDR3 having a sequence Q(Q/H)FWGTPYT (SEQ ID NO:41) and a V_(H) region that has a CDR3 having a sequence NRGDIYYDFTYA(M/F)DX₁ (SEQ ID NO:42), wherein X₁ is I, Q, Y, or S.
 2. The isolated anti-PcrV antibody of claim 1, wherein the V_(H) V-segment as at least 80% identity to the human VH1-18 subclass V-segment or to the human VH3-30.3 V segment and the V_(L) V-segment has at least 80% identity to a human germline Vkappa I or Vkappa III sequence, or at least 80% identity to a human germline Vlambda sequence.
 3. The isolated anti-PcrV antibody of claim 2, wherein the V_(H) region comprises a FR4 that has at least 90% identity to the FR4 region of the human JH3 or human JH6 segment and the V_(L) region comprises a FR4 that has at least 90% identity to the FR4 region of the human JK2 germline gene segment or at least 90% identity to the JL2 germline sequence.
 4. The isolated anti-PcrV antibody of claim 3, wherein the FR4 of the V_(H) region has the sequence WGQGTX₂VTVSS (SEQ ID NO:45), wherein X₂ is T or M; and the FR4 of the V_(L) region has the sequence FGQGTKLEIK (SEQ ID NO:47) or FGGGTKLTVL (SEQ ID NO:48).
 5. The isolated anti-PcrV antibody of claim 1, wherein the antibody is a Fab′.
 6. The isolated anti-PcrV antibody of claim 1, wherein the antibody is PEGylated.
 7. The isolated anti-PcrV antibody of claim 1, wherein the antibody is a di-PEGylated Fab′.
 8. A composition comprising the isolated anti-PcrV antibody of claim 1 and a pharmaceutically acceptable carrier.
 9. An isolated anti-PcrV antibody that selectively binds PcrV, wherein the antibody comprises: a V_(H) region having a CDR3 having a sequence NRGDIYYDFTYAMDI (SEQ ID NO:99), a CDR2 sequence VISYDGSEKWYADSVKG (SEQ ID NO:57), and a CDR1 sequence NYPMH (SEQ ID NO:54); and a V_(L) region.
 10. The isolated anti-PcrV antibody of claim 9, wherein the V_(H) region comprises the amino acid sequence of the V-segment region of SEQ ID NO:26.
 11. The isolated anti-PcrV antibody of claim 10, wherein the V_(H) region comprises the amino acid sequence of the V-segment region of SEQ ID NO:26.
 12. The isolated anti-PcrV antibody of claim 9, wherein the antibody is a Fab′.
 13. The isolated anti-PcrV antibody of claim 9, wherein the antibody is PEGylated.
 14. The isolated anti-PcrV antibody of claim 9, wherein the antibody is a di-PEGylated Fab′.
 15. A composition comprising the isolated anti-PcrV antibody of claim 9 and a pharmaceutically acceptable carrier.
 16. An isolated anti-PcrV antibody that selectively binds PcrV, wherein the antibody comprises: a V_(L) region that comprises a CDR3 having a sequence QHFWGTPYT (SEQ ID NO:110), a CDR2 sequence DASTLQS (SEQ ID NO:73), and a CDR1 sequence RASEGVDRWLA (SEQ ID NO:69); and a V_(H) region.
 17. The isolated anti-PcrV antibody of claim 16, wherein the V_(L) region comprises the amino acid sequence of the V-segment of SEQ ID NO:24.
 18. The isolated anti-PcrV antibody of claim 17, wherein the V_(L) region comprises the amino acid sequence set forth in SEQ ID NO:24.
 19. The isolated anti-PcrV antibody of claim 16, wherein the antibody is a Fab′ fragment.
 20. The isolated anti-PcrV antibody of claim 16, wherein the antibody is a di-PEGylated Fab′. 